Segmentable container and method of segmenting substance contained in container

ABSTRACT

Provided are a simple, quick, and low-processing cost method capable of reliably separating part of an accommodated substance accommodated in a vessel only by simple mechanical operation while maintaining a hermetically-sealed state without any contact with an outside atmosphere, as well as a vessel with which the method may be used. A separable vessel comprises a first vessel portion, a second vessel portion which is contiguous with the first vessel portion, a fracture-inducing portion formed between the first vessel portion and the second vessel portion, and a self-fusing material provided on an outer surface so as to cover the fracture-inducing portion; and may contain an accommodated substance therein.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional Application of patent application Ser.No. 14/387,116, filed on Sep. 22, 2014, which is a 371 application ofApplication No. PCT/JP2013/053241, filed on Feb. 12, 2013, which isbased on Japanese Application No. 2012-081233, filed on Mar. 30, 2012,the entire contents of which are hereby incorporated by reference.

TECHNICAL FIELD

The present invention relates to a method for separating and collectingan accommodated substance or part thereof from a vessel-shaped structureaccommodating one or more of a liquid, a solid, a gas, and a dispersionsystem without contact with outside air or without leakage to theoutside, and a vessel and device suitable for the method.

Particularly, the present invention relates to a method for easilyseparating and collecting an accommodated substance or part thereof froma vessel-shaped structure accommodating one or more of a liquid, asolid, a gas, and a dispersion system in a hermetically-sealed statewhile maintaining the hermetically-sealed state, and a vessel and devicesuitable for the method.

The present invention can be used to separate and collect part or all ofa liquid, a solid, a gas, or the like accommodated in one or more spacesin a vessel while maintaining a hermetically-sealed state. The presentInvention is useful in food and medical fields requiring asepticmanipulation, manufacturing and processing fields handling hazardoussubstances or radioactive substances, and semiconductor and mi erodevice manufacturing fields requiring a dust-free environment.

BACKGROUND ART

As structures (specifically, hermetically-sealed vessels) for storing anaccommodated substance in a hermetically-sealed state in order to avoidchemical actions such as oxidation by an outside atmosphere, diffusionof hazardous substances, contaminants, or microorganisms contained invessels to the outside, or entry of hazardous substances, contaminants,or microorganisms into vessels from the outside, cans, bottles, ampules,vials, and hermetically-sealed packages using resin films or sheets areconventionally used.

A typical example of a structure, from which part of an object substanceaccommodated therein in a hermetically-sealed state can be separatedwhile being the hermetically sealed state, includes a sheet ofpharmaceutical tablets disclosed in JP-A-8-206177 (Patent Document 1)and JP-A-10-248905 (Patent Document 2). In the case of a structure suchas a sheet of tablets, accommodated substances (tablets) are previouslyhermetically sealed in their respective independent spaces, andtherefore do not come into contact with each other in the structure.

JP-A-2011-229488 (Patent Document 3) discloses a hermetically-sealednucleic acid amplification reaction system in which a nucleic acidamplification reaction is performed in a droplet of a nucleic acidamplification reaction liquid encapsulated by a droplet encapsulatingmedium while the droplet is moved in a vessel filled with the dropletencapsulating medium insoluble or poorly soluble in the nucleic acidamplification reaction liquid.

JP-A-2011-232260 (Patent Document 4) discloses a hermetically-sealedmanipulation system in which a substance in a droplet of an aqueousliquid encapsulated by a gel-state droplet encapsulating medium ismanipulated while the droplet is moved in a vessel filled with thegel-state droplet encapsulating medium insoluble or poorly soluble inthe aqueous liquid.

PRIOR ART DOCUMENTS Patent Documents

Patent Document 1: J-PA-8-206177

Patent Document 2: JP-A-10-248905

Patent Document 3: JP-A-2011-229488

Patent Document 4: JP-A-2011-232260

SUMMARY OF THE INVENTION Problems to be Solved by the Invention

When used only for storage of an object substance to be separated, astructure may be configured like the sheet of tablets disclosed in thePatent Document 1 and the Patent Document 2 so that object substances(tablets) are accommodated in their respective independent spaces.

However, when being not just a storage vessel but a vessel used topreviously subject an object substance to be separated to the process ofphysical, chemical, and/or biological manipulation, a structure isrequired to allow both an object substance and a manipulation medium tobe present in the same vessel so that the object substance can come intocontact with the manipulation medium that provides a field forperforming the above-described manipulation.

For example, in a structure for performing both physical, chemical, orbiochemical manipulation and collection of an object substance subjectedto the manipulation, both a manipulation medium for performing physical,chemical, or biochemical manipulation and a collection medium forcollecting a final product may be present in the same vessel. In thecase of such a structure, even after the completion of variousmanipulations and collection, an object substance after themanipulations and a medium used for the manipulations are present in thesame interior space. Therefore, in order to prevent unnecessary mixingof both present in the interior space, there is a case where only acollection medium, in which the object substance after the manipulationsis present, is required to be separated.

When such separation is performed by, for example, simply cutting thestructure between a part accommodating a manipulation medium(manipulation portion) and a part accommodating a collection medium(collection portion), both the manipulation portion and the collectionportion separated from each other have an open end so that theaccommodated substance is exposed to an outside atmosphere. Even wheneach open end is covered with airtight stoppers immediately after theseparation, it is impossible to avoid contact between the accommodatedsubstance and an outside atmosphere or diffusion of the accommodatedsubstance to an outside atmosphere.

Therefore, in the above case, there is a case where part of theaccommodated substance is further required to be separated without anycontact with an outside atmosphere. This applies to, for example, a casewhere a reaction product obtained by a biochemical reaction performed inthe structure is one that is easily oxidized by oxygen contained in anoutside atmosphere, a case where the reaction product is one that iseasily contaminated by exposure to an outside atmosphere, or a casewhere the reaction product is one that contaminates an outsideatmosphere.

It is considered that, as an example of satisfying the aboverequirement, provided is a structure including a manipulation portionaccommodating a manipulation medium and a collection portionaccommodating a collection medium for an object substance aftermanipulation, wherein a physical separation system with an opening andclosing system, such as a shutter, is formed between the manipulationportion and the collection portion. However, when the structuresatisfying the above requirement is required to be a small vessel suchas a microdevice, it is not easy for the vessel to have such acomplicated system.

Also in the case of each of the vessels disclosed in Patent Document 3and Patent Document 4, a nucleic acid amplification reaction productproduced in the vessel or a substance after the completion ofmanipulation in the vessel cannot be taken out from the vessel whilebeing maintained in a hermetically-sealed state.

Therefore, an object of the present invention is to provide simple,quick, and low-processing cost means capable of reliably separating part(for example, a collection liquid) of an accommodated substance (forexample, a manipulation medium for performing physical, chemical, and/orbiochemical treatment and a collection liquid containing a targetsubstance) accommodated in a vessel only by simple mechanical operationwhile maintaining a hermetically-sealed state without any contact withan outside atmosphere.

Means for Solving to the Problems

The present inventors have intensively studied, and as a result, foundthat the above object of the present invention can be achieved byaccommodating a substance to be accommodated in a vessel having afracture-inducing portion formed in a position where the vessel shouldbe separated and a self-fusing material provided so as to cover thefracture-inducing portion. This finding has led to the completion of thepresent invention.

The present invention includes the following.

(1) A separable vessel comprising:

a fracture-inducing portion formed in a position where fracture shouldbe caused to separate the vessel into a first vessel portion and asecond vessel portion; and

a self-fusing material provided on an outer surface so as to cover thefracture-inducing portion.

(2) The vessel according to the above (1), containing an accommodatedsubstance therein.

(3) The vessel according to the above (2), being a manipulation vesselfor subjecting a sample containing an object component to apredetermined manipulation therein, wherein

the first vessel portion is a manipulation portion for subjecting asample containing an object component to a predetermined manipulation,

the second vessel portion is a collection portion for collecting atarget substance from the manipulation portion, and

the accommodated substance is a manipulation medium selected from thegroup consisting of a liquid, a solid, a gas, and a dispersion system,as a field for performing manipulation to which the object component isto be subjected.

(4) The vessel according to the above (3), wherein the manipulationportion comprises a column for chromatography, and the manipulationmedium comprises a filling material for chromatography and a developingsolvent.

A specific example of an embodiment of the above (4) is shown in FIG.1(1).

(5) The vessel according to the above (3), having a tubular shape,wherein the manipulation medium is a multi-layered object in whichlayers of an aqueous liquid and a gel are alternately stacked in alongitudinal direction.

A specific example of an embodiment of the above (5) is shown in FIG.1(2).

(6) The vessel according to the above (3), wherein the manipulationmedium comprises a droplet encapsulating medium and an encapsulatedaqueous droplet.

A specific example of an embodiment of the above (6) is shown in FIG. 2.

(7) The vessel according to any one of the above (1) to (6), furthercomprising a protective member on an outer surface of the self-fusingmaterial.

(8) The vessel according to any one of the above (1) to (7), wherein theself-fusing material has a thickness of 0.01 to 5 mm per 1 cm² of areaof a plane within an outer periphery of the vessel.

(9) The vessel according to any one of the above (1) to (8), wherein thefracture-inducing portion is a portion having been subjected totreatment to reduce a wall thickness of the vessel and/or treatment toreduce the material strength of the vessel.

A preferred example of the portion having been subjected to treatment toreduce a wall thickness of the vessel is a groove (fracture-inducinggroove) formed in the surface of the vessel. The treatment to reduce thematerial strength of the vessel does not include the treatment to reducea wall thickness of the vessel.

The fracture-inducing groove may have a depth 0.3 to 0.6 times thethickness of the vessel.

(10) The vessel according to any one of the above (1) to (9), whereinthe self-fusing material is selected from the group consisting ofisobutylene-isoprene copolymers, ethylene-propylene-diene copolymers,polyisobutylene, paraffin, polyvinyl acetate, polyurethane, polydimethylsiloxane, ethylene propylene copolymers, hydrogel polymers,(meth)acrylic acid ester copolymers, silicone rubber, and naturalrubber.(11) The vessel according to any one of the above (1) to (10), whereinthe self-fusing material is a thermoplastic resin having a glasstransition temperature of 50° C. to 180° C.(12) The vessel according to the above (11), wherein the thermoplasticresin is selected from the group consisting of polyethylene,polypropylene, polystyrene, ethylene-vinyl acetate copolymers,polyacetal, polymethyl methacrylate, polyvinyl alcohol, polyvinylchloride, vinyl chloride-vinyl acetate copolymers, vinylchloride-acrylic acid ester copolymers, polyvinylidene chloride, andvinylidene chloride-acrylic acid ester copolymers.(13) A manipulation device for manipulating an object component in avessel, comprising:

the vessel according to any one of the above (2) to (12);

magnetic particles that should capture and transport an objectcomponent; and

magnetic field application means for applying a magnetic field to thevessel so that the magnetic particles can be moved from an inside of thefirst vessel portion to an inside of the second vessel portion.

(14) A method for separating a substance accommodated in a vessel, thevessel being a separable vessel comprising: a fracture-inducing portionformed in a position where fracture should be caused to separate thevessel into a first vessel portion and a second vessel portion; and aself-fusing material provided on an outer surface so as to cover thefracture-inducing portion, and the vessel containing an accommodatedsubstance therein,

the method comprising subjecting the vessel to the following steps:

(i) applying an external force to the vessel to cause fracture in aposition of the fracture-inducing portion so that the first vesselportion and the second vessel portion are separated from each other toform fracture openings of the respective vessel portions but areconnected to each other through the self-fusing material;

(ii) pulling the first vessel portion and the second vessel portion awayfrom each other to extend the self-fusing material;

(iii) fusing the extended self-fusing material together so that a spacebetween the first vessel portion and the second vessel portion isblocked to separate the accommodated substance; and

(iv) cutting a fused part of the self-fusing material to separate thevessel into a first separated structure that includes the first vesselportion whose fracture opening is closed by the self-fusing material andthat contains one of the separated parts of the accommodated substance,and a second separated structure that includes the second vessel portionwhose fracture opening is closed by the self-fusing material and thatcontains the other separated part of the accommodated substance.

(15) The method according to the above (14), wherein the external forcein the step (i) is a twisting force around an axis in a direction inwhich the first vessel portion and the second vessel portion are to bepulled away from each other in the step (ii).(16) The method according to the above (15), wherein the twisting forceis 8 to 11 cN·m.(17) The method according to any one of the above (14) to (16), whereinin the steps (iii) and (iv), the fusion of the extended self-fusingmaterial together and the cutting of the fused part are performed bytwisting the first vessel portion and the second vessel portion aroundan axis in a direction in which the first vessel portion and the secondvessel portion have been pulled away from each other.

A specific example of an embodiment of the above (17) is shown in FIG.3.

(18) The method according to any one of the above (14) to (16), whereinthe extended self-fusing material is fused together by externallypinching with pressure-bonding means in the step (iii), and the fusedpart is cut with cutting means in the step (iv).

(19) The method according to the above (18), wherein thepressure-bonding means and the cutting means are separately prepared.

A specific example of an embodiment of the above (19) is shown in FIG.4.

(20) The method according to the above (18), wherein thepressure-bonding means comprises a pair of pressure-bonding members; and

the cutting means is prepared in such a manner that a flat plate-shapedcutting blade is provided so as to be able to penetrate into one memberof the pair of pressure-bonding members, and the cutting of the fusedpart in the step (iv) is performed by allowing the flat plate-shapedcutting blade to penetrate the one of the pair of pressure-bondingmembers.

A specific example of an embodiment of the above (20) is shown in FIG.5.

(21) The method according to any one of the above (14) to (20), whereinthe vessel to be subjected to the steps (i) to (iv) further comprises aprotective member on an outer surface of the self-fusing material.

(22) The method according to any one of the above (14) to (21), whereinthe self-fusing material has a thickness of 0.01 to 5 mm per 1 cm² ofarea of a plane within an outer periphery of the vessel.

(23) The container according to any one of the above (14) to (22) fwherein the fracture-inducing portion is a portion having been subjectedto treatment to reduce a wall thickness of the vessel and/or treatmentto reduce the material strength of the vessel.(24) The method according to any one of the above (14) to (23), whereinthe self-fusing material is selected from the group consisting ofisobutylene-isoprene copolymers, ethylene-propylene-diene copolymers,polyisobutylene, paraffin, polyvinyl acetate, polyurethane, polydimethylsiloxane, ethylene propylene copolymers, hydrogel polymers,(meth)acrylic acid ester copolymers, silicone rubber, and naturalrubber.(25) The method according to any one of the above (14) to (24), whereinthe self-fusing material is a thermoplastic resin having a glasstransition temperature of 50° C. to 180° Ct(26) The method according to the above (25), wherein the thermoplasticresin is selected from the group consisting of polyethylene,polypropylene, polystyrene, ethylene vinyl acetate copolymers,polyacetal, polymethyl methacrylate, polyvinyl alcohol, polyvinylchloride, vinyl chloride-vinyl acetate copolymers, vinylchloride-acrylic acid ester copolymers, polyvinylidene chloride, andvinylidene chloride-acrylic acid ester copolymers.(27) The method according to any one of the above (14) to (26), wherein

the vessel is a manipulation vessel for subjecting a sample containingan object component to a predetermined manipulation therein,

the first vessel portion is a manipulation portion for subjecting asample containing an object component to a predetermined manipulation,

the second vessel portion is a collection portion for collecting atarget substance from the manipulation portion, and

the accommodated substance is a manipulation medium selected from thegroup consisting of a liquid, a solid, a gas, and a dispersion system,as a field for performing manipulation to which the object component isto be subjected,

the method further comprising, prior to the step (i), subjecting themanipulation vessel to the step of subjecting the sample to apredetermined manipulation and collecting the target substance.

(28) The method according to the above (27), wherein the manipulationportion comprises a column for chromatography, and the manipulationmedium comprises a filling material for chromatography and a developingsolvent.

A specific example of an embodiment of the above (28) is shown in FIG.4.

(29) The method according to the above (27), wherein the manipulationvessel has a tubular shape, and the manipulation medium is amulti-layered object in which layers of an aqueous liquid and a gel arealternately stacked in a longitudinal direction.

A specific example of an embodiment of the above (29) is shown in FIG.7.

(30) The method according to the above (27), wherein the manipulationmedium comprises a droplet encapsulating medium and an encapsulatedaqueous droplet.

A specific example of an embodiment of the above (30) is shown in FIG.8.

(31) The method according to the above (29) or (30), wherein themanipulation portion has an openably-closed sample supply portion forsupplying a sample into the manipulation vessel, and after a step ofsupplying the sample, the accommodated substance is maintained in acompletely hermetically-sealed state until the step (iv) is finished.

Effects of the Invention

According to the present invention, a simple, quick, and low-processingcost method can be provided which is capable of reliably separating part(for example, a collection liquid) of an accommodated substance (forexample, a manipulation medium for performing physical, chemical, and/orbiochemical treatment and a collection liquid containing a targetsubstance) accommodated in a vessel only by simple mechanical operationwhile maintaining a hermetically-sealed state without any contact withan outside atmosphere, and a vessel that can implement such a method canbe provided.

According to the present invention, the production cost of the vessel islow because the vessel does not need to have a complicated opening andclosing system. Further, part of the vessel can be separated andcollected by a simple system, and therefore the vessel can be applied toa miniaturized device.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1(1) and 1(2) are vertical sectional views of examples of a vesselaccording to the present invention.

FIG. 2 is a vertical sectional view of another example of the vesselaccording to the present invention.

FIG. 3 shows one example of a separation method according to the presentinvention.

FIG. 4 shows another example of the separation method according to thepresent invention.

FIG. 5 shows a modified embodiment of a separation system shown in FIG.4.

FIG. 6 shows another example of the separation method according to thepresent invention.

FIG. 7 shows an example of performing the method according to thepresent invention with the use of a device using a manipulation tube.

FIG. 8 shows an example of performing the method according to thepresent invention with the use of a device using a plate-shaped vessel.

FIG. 9 is a vertical sectional view of a vessel tested in ExperimentalExample 1.

FIG. 10 is a graph showing a relationship between the depth of afracture-inducing groove and a rotational torque that causes a vessel tobe separated due to stress concentration on the fracture-inducinggroove.

DESCRIPTION OF REFERENCE SIGNS

-   -   1: vessel (manipulation vessel)    -   a: first vessel portion    -   b: second vessel portion    -   X: self-fusing material    -   A: manipulation portion    -   B: collection portion    -   3 l: aqueous liquid layer    -   3 g, 2 g: gel layer    -   3 d: aqueous droplet    -   5: droplet encapsulating medium    -   6: fracture-inducing groove    -   11 a, 11 b: fracture opening    -   12: open end (sample supply portion)    -   16: protective member    -   31: pressure-bonding member    -   32: cutting means    -   41, 42: flat plate-shaped cutting blade (41: cutter main body,        42: cutting edge)    -   61: magnetic particles    -   63: magnetic field applying means (magnet)

MODE FOR CARRYING OUT THE INVENTION

1. Basic Structure of Vessel

Examples of a vessel according to the present invention are shown inFIGS. 1 and 2. FIGS. 1 and 2 are sectional views of the vessel. A vessel1 according to the present invention includes a first vessel portion aand a second vessel portion b. The first vessel portion a and the secondvessel portion b are continuous and integral with each other, and asingle interior space is created within the vessel. A fracture-inducingportion 6 (fracture-inducing groove) is formed in the outer surface ofthe vessel. The fracture-inducing groove 6 is located at the boundarybetween the first vessel portion a and the second vessel portion b.Further, a self-fusing material X is provided on the outer surface ofthe vessel so as to cover the fracture-inducing groove 6.

The shape of the vessel is not particularly limited. For example, thesectional shape of the vessel may be an almost circle, a segment of acircle, a polygon, or the like. More specifically, the vessel may have,for example, a blind tube shape as shown in FIG. 1(1) and FIG. 1(2), ora deformed rectangular shape as shown in FIG. 2, or another shape.

The vessel 1 may have an open end 12 on the first vessel portion a-side.Part or whole of the open end 12 may be openably closed. FIG. 1(2) showsan example in which part of the open end is openably closed. In the caseof this embodiment, the use of a septum 14 having the function of acheck valve makes it possible to supply a sample by puncture with aninjection needle in a state close to a hermetically-sealed state.Further, FIG. 2 shows an example in which whole of the open end isopenably closed. In the case of this embodiment, a lid 15 that coversthe open end 12 can be used.

Closing the open end 12 is preferred in that a complete closed systemcan be constructed in the vessel 1.

The fracture-inducing portion (fracture-inducing groove 6 in theexamples shown in the drawings) is located at the boundary between thefirst vessel portion a and the second vessel portion b. Thefracture-inducing portion is a portion subjected to stress concentrationdue to an appropriate external force applied from the outside of thevessel. The stress concentration effectively induces fracture. Thefracture-inducing portion is preferably formed over the entire outerperiphery of the vessel. Preferably, the fracture-inducing portion maybe formed to have such a strength that, when a twisting force is appliedas an external force from the outside of the vessel to cause fracture,fracture occurs at about 8 to 11 cN·m.

The fracture-inducing portion may be embodied as a portion having beensubjected to treatment to reduce the wall thickness of the vessel as inthe case of the fracture-inducing groove 6 illustrated in the drawing,or may be embodied as a portion having been subjected to treatment tolocally reduce the material strength of the vessel.

The cross-section of the fracture-inducing groove may have either a U orV shape. The size of the groove can be appropriately determined by thoseskilled in the art depending on the shape of the vessel, the thicknessof the vessel, the type of external force-applying means, etc, so thatfracture can be effectively induced. For example, the depth of thefracture-inducing groove may be 0.3 to 0.6 times the thickness of thevessel (for example, 0.1 to 10 mm, preferably 0.5 to 3.0 mm). If thedepth exceeds the above range, an external force required for separationcan be made small, but because of that, durability tends to be aproblem. If the depth is less than the above range, a great externalforce is required at the time of separating the vessel. In addition, itis difficult to effectively concentrate stress on the fracture-inducinggroove, which tends to cause deformation of the whole vessel. When thevessel is made of a soft material, the fracture-inducing groove may beformed to be relatively shallow. In the present invention, thefracture-inducing groove is preferably formed to have a V-shapedcross-section. In this case, the fracture-inducing groove having aV-shaped cross-section is formed so that the angle of the V shape ispreferably 15° to 90°, for example, 60°.

An example of the treatment to locally reduce the material strength ofthe vessel includes treatment in which the mechanical strength of thematerial of the vessel is reduced (the material of the vessel isfatigued) by applying physical stress, electricity, or radiation to thematerial of part of the vessel where the f ruction-inducing portionshould be formed. Such treatment makes it possible to embody thefracture-inducing portion as, for example, a portion having a pluralityof fine cracks. An example of the treatment also includes treatment inwhich the material of part of the vessel where the fracture-inducingportion should be formed is brought into contact with an organic solventto be swelled. Such treatment makes it possible to embody thefracture-inducing portion as a portion having a large number ofmicropores or a softened portion.

Another example of the treatment to locally reduce the material strengthof the vessel includes treatment to chemically change the material ofthe vessel to produce a low-strength product. An example includestreatment in which the material of part of the vessel where thefracture-inducing portion should be formed is brought into contact andis allowed to react with a corrosive chemical agent. Such treatmentmakes it possible to embody the fracture-inducing portion as a portionmade of a corrosion product.

The depth of the portion having reduced material strength from thesurface of the vessel may be 0.3 to 0.6 times the thickness of thevessel as in the case of the above-described fracture-inducing groove.

A material of the vessel is not particularly limited. Examples of thematerial include resin materials such as polypropylene, polyethylene,fluorine resins (e.g., Teflon (registered trademark)), polyvinylchloride, polystyrene, polycarbonate, acrylonitrile butadiene copolymers(ABS resins), acrylonitrile styrene copolymers (AS resins), acrylicresins, polyvinyl acetate, polyethylene terephthalate, and cyclicpolyolefins. Alternatively, the material may be ceramic, glass,silicone, or metal.

An accommodated substance may be contained in the interior space createdin the vessel. The form of the accommodated substance is notparticularly limited, and can be appropriately determined by thoseskilled in the art depending on the intended use of the structure. Thatis, as the accommodated substance, one or more are arbitrarily selectedfrom the group consisting of a liquid, a solid, a gas, and a dispersionsystem.

The vessel 1 according to the present invention may be used for thepurpose of manipulating an object substance therein. When used as avessel for manipulating an object substance, the vessel 1 according tothe present invention may be particularly sometimes referred to as amanipulation vessel. In the manipulation vessel 1, a portioncorresponding to the first vessel portion a may be sometimes referred toas a manipulation portion A, and a portion corresponding to the secondvessel portion b may be sometimes referred to as a collection portion B.The manipulation vessel 1 may have a sample supply portion forexternally supplying a sample containing an object component to foemanipulated. The sample supply portion may be the open end 12 providedon the manipulation portion A side. As has already been described, theopen end 12 may be open or may be openably closed from the viewpoint ofhermeticity.

The accommodated substance in the manipulation vessel 1 includes amanipulation medium as a field for performing manipulation to which anobject component is to be subjected. For example, when the manipulationportion A is a column for chromatography as illustrated in FIG. 1(1),the manipulation medium may comprise a filling material forchromatography and a developing solvent 3 c. Further, for example, whenthe manipulation vessel 1 has a tubular shape as illustrated in FIG.1(2), the manipulation medium may be a multi-layered object in whichaqueous liquid layers 3 l and gel layers 3 g and 2 g are alternatelystacked in a longitudinal direction. Further, for example, when themanipulation vessel 1 has such a shape as illustrated in FIG. 2, themanipulation medium may comprise a droplet encapsulating medium 5 and anaqueous droplet 3 d encapsulated thereby and/or an aqueous droplet 3 d′held thereby. The accommodated substance in the manipulation vessel 1will be described later in detail in Section 4.

[2. Self-Fusing Material]

In the present invention, the self-fusing material refers to a substancethat easily deforms by being present in a semi-solid state and that hasthe property of mixing and fusing together toy pressure contact of theself-fusing material (self-fusibility). Due to such a property, theself-fusing material can fill a narrow gap and can come into closecontact with an object without any gap even when an adhesive or apressure-sensitive adhesive is not used. Therefore, the self-fusingmaterial can come into close contact with the open end, therebyhermetically sealing the open end.

The self-fusibility may be, for example, one developed at ordinarytemperature (e.g., 20° C.±15° C.) or one developed by heating (e.g., at50 to 180° C. or 50 to 150° C.).

The self-fusing material is widely known to those skilled in the art,and is not particularly limited. For example, the self-fusing materialmay be selected from the group consisting of isobutylene-isoprenecopolymers (butyl rubber), ethylene-propylene-diene copolymers,polyisobutylene, paraffin, polyvinyl acetate, polyurethane,polydimethylsiloxane, ethylene propylene copolymers, hydrogel polymers,(meth)acrylic acid ester copolymers (which may be in the form of(meth)acrylic pressure-sensitive adhesive or acrylic foam), siliconerubber, and natural rubber. These self-fusing materials may be usedsingly or in combination of two or more thereof. The above-mentionedself-fusing materials are preferred in point of being capable of havingself-fusibility at ordinary temperature. Among the above-mentionedself-fusing materials, for example, an isobutylene-isoprene copolymer ispreferably used in the present invention.

On the other hand, an example of the self-fusing material in whichself-fusibility is developed by heating includes a thermoplastic resinhaving a glass transition temperature of 50° C. to 180° C. or 50 to 150°C. Such a thermoplastic resin may be selected from the group consistingof polyethylene, polypropylene, polystyrene, ethylene vinyl acetatecopolymers, polyacetal, polymethyl methacrylate, polyvinyl alcohol,polyvinyl chloride, vinyl chloride-vinyl acetate copolymers, vinylchloride-acrylic acid ester copolymers, polyvinylidene chloride, andvinylidene chloride-acrylic acid ester copolymers. These self-fusingmaterials may be used singly or in combination of two or more thereof.Further, the self-fusing material in which self-fusibility is developedby heating may be used in combination with the above-described substancehaving self-fusibility at ordinary temperature.

As shown in FIG. 1, the self-fusing material X forms a layer on theouter surface of the vessel-shaped structure 1 so as to cover thefracture-inducing groove 6 formed between the first vessel portion a andthe second vessel portion b and its surroundings. For example, the layercan be formed by preparing a tape-shaped self-fusing material andwrapping the tape-shaped self-fusing material around the outerperipheral surface of the vessel so that the self-fusing material isintegrated with the vessel by self-fusion. The layer of the self-fusingmaterial shall have such a thickness that a separation method accordingto the present invention can be achieved, and the thickness of the layeris not particularly limited because the required thickness of the layervaries depending on the area of a plane within the outer periphery ofpart of the vessel that should be covered with the layer. However, thethickness of the layer may be, for example, 0.01 to 5 mm or 0.1 to 5 mmper 1 square centimeter of area of a plane within the outer periphery ofthe vessel. Here, the area of a plane within the outer periphery of thevessel refers to the area of a plane enclosed by the outer periphery ofthe cross-section of the vessel not including the fracture-inducinggroove. More specifically, the layer of the self-fusing material mayhave a thickness of 0.001 to 3 mm or 0.1 to 0.5 mm. If the thicknessexceeds the above range, there is a tendency that an excessive force isrequired for separating the vessel-shaped structure or the need forexcessively strongly providing a protective member, which will bedescribed later, arises. If the thickness is less than the above range,there is a tendency that a membrane of the self-fusing material iseasily broken when the vessel-shaped structure is separated or amembrane of the self-fusing material closing the separated vessel-shapedstructure is too thin.

Means for forming a layer of the self-fusing material on the vessel isnot limited to taping with a tape-shaped self-fusing material. Forexample, a layer of the self-fusing material can be formed by dissolvingthe self-fusing material in a volatile organic solvent and applying thesolution onto a target part of the vessel. For example, butyl rubber isdissolved in various volatile organic solvents such as toluene, xylene,and tetrahydrofuran, and has high viscosity in a high concentration, andtherefore a layer of the self-fusing material can be formed byapplication with high reproducibility. After being dried, the layer ofthe self-fusing material exhibits the same self-fusibility as thatformed by the raping method.

In the vessel 1 of the present invention, a protective member 16 forprotecting the self-fusing material X may be further provided on theouter surface of the self-fusing material X. The protective member maybe provided for the purpose of preventing the contamination of thesurface of the self-fusing material and preventing cold flow that is aphenomenon unique to the self-fusing material. Further, when two or morevessels are gathered together, the protective member also prevents thevessels from adhering to each other due to contact between theself-fusing material parts. The protective member may be made of anymaterial as long as such purposes can be achieved. For example, a thinfilm that can be easily broken may be used as the protective member, andthe self-fusing material can be covered by attaching the thin film tothe surface of the self-fusing material. Specific examples of such athin film include wafer paper, paper, resin thin films, and metal thinfilms typified by aluminum foil. Further, the thin film may have abreaking guide line (perforation) so as to be broken at a desiredposition.

[3. Method for Separating Accommodated Substance in Vessel]

In the present invention, in order to separate the accommodatedsubstance in the vessel, the vessel itself containing the accommodatedsubstance is separated. In the present invention, the vessel isseparated through the step (i) of causing fracture in thefracture-inducing portion, the step (ii) of extending the self-fusingmaterial, the step (iii) of separating the accommodated substance, andthe step (iv) of separating the first vessel portion and the secondvessel portion from each other. The steps of the separation methodaccording to the present invention are schematically shown in FIGS. 3and 4.

In the step (i), an external force is applied to the vessel toconcentrate stress on the fracture-inducing groove 6 so that, asillustrated in FIG. 3(i) or FIG. 4(i), fracture is caused and fractureopenings 11 a and 11 b are formed. The external force shall be such aforce that the fracture-inducing groove 6 can be subjected to stressconcentration to the extent that fracture occurs. For example, theexternal force may be a force applied in a direction almost parallel tothe fracture-inducing groove 6, a force to pull the first vessel portionand the second vessel portion away from each other, a twisting forcearound an axis in a direction in which the first vessel portion and thesecond vessel portion are pulled away from each other, or the resultantof a force to pull the first vessel portion and the second vesselportion away from each other and a twisting force around an axis in adirection in which the first vessel portion and the second vesselportion are pulled away from each other. In the present invention, inconsideration of automatically performing the steps for separation, thefracture-inducing portion is preferably fractured by a twisting force.For example, when the steps for separation are automatically performed,a twisting force can be generated by fixing the first vessel portion andthe second vessel portion with their respective fixtures (fixtures 91and 92 of FIG. 9 to be described later) and, without moving one of thefixtures (for example, the fixture fixing the first vessel portion),rotating the other fixture (for example, the fixture fixing the secondvessel portion) using rotary means such as a motor. When the vessel hasa circular cross-section, a contact surface between the vessel and thefixture may be subjected to anti-slip treatment.

The magnitude of the twisting force is not particularly limited andvaries depending on the material of the vessel, the thickness of thevessel, or the type of the fracture-inducing portion (for example, inthe case of the fracture-inducing groove, the magnitude of the twistingforce varies depending on the depth of the groove, and in other cases,the magnitude of the twisting force varies depending on the materialstrength of the fracture-inducing portion of the vessel). For example,the magnitude of the twisting force is 8 to 11 cN·m. If the forceexceeding the above range is required, there is a tendency that thedesign of the vessel is less likely to effectively cause stressconcentration on the fracture-inducing portion. When the force is lessthan the above range, there is a tendency that fracture is less likelyto effectively occur.

In the step (ii), as illustrated in FIG. 3(ii) and FIG. 4(ii), the firstvessel portion a and the second vessel portion b are pulled away fromeach other to create a sufficient gap between both the vessel portions.The first vessel portion a and the second vessel portion b can be easilypulled away from each other by pulling one of the vessel portions orpulling both the vessel portions in opposite directions. This makes itpossible to extend the self-fusing material X. When the self-fusingmaterial X is further covered with the protective member 16, theself-fusing material X is extended and the protective member 16 is tornby pulling both the vessel portions a and b away from each other. Thesurface having high self-fusibility of the extended self-fusing materialX is exposed through a tear in the protective member 16. That is, thesurface of the self-fusing material can have high self-fusibility byextending the self-fusing material in the step (ii).

The first vessel portion a and the second vessel portion b are stillconnected by the self-fusing material X, whereas the self-fusingmaterial X is extended. Therefore, a membrane of the extendedself-fusing material X also allows the space in the vessel including thegap created between both the vessel portions a and b to remaincompletely isolated from an outside atmosphere. The space in the vesselincluding the gap created between both the vessel portions is separatedby the present invention, but a substance allowed to be accommodated inthe space as an accommodated substance is not particularly limited, andmay be any one selected from the group consisting of a liquid (which maybe either aqueous or non-aqueous), a gas and a dispersion system.According to the method of the present invention, it is possible,whatever substance is accommodated in a part to be separated, toseparate the substance without leakage to the outside.

It is to be noted that when the temperature of a manipulationenvironment upon performing the step (ii) is lower than a temperature atwhich the self-fusing material develops self-fusibility (especially,when a thermoplastic resin is used), appropriate heating may beperformed to a temperature at which self-fusion can be achieved.

In the step (iii), the self-fusing material whose surface having highself-fusibility has been exposed by extension is fused together. Amethod for fusing the self-fusing material is not particularly limitedas long as the accommodated substance can be separated by blocking thespace between the first vessel portion a and the second vessel portionto so that the interior space of the vessel, which has been a singlespace so far, is separated.

An example of the method is as follows. As shown in FIG. 3(iii), atwisting force is applied around an axis in a direction in which thefirst vessel portion a and the second vessel portion b are pulled awayfrom each other. The twisting force may be applied by fixing one of thefirst vessel portion a and the second vessel portion b and turning theother vessel portion or by turning the first vessel portion a and thesecond vessel portion b in opposite directions. For example, one or bothof the vessel portions a and b may be turned once to twice. Thismanipulation makes it possible to twist the self-fusing material X,whose surface has high self-fusibility, between both the vessel portionsa and b and to self-fuse the self-fusing material X in a twisted stateso that the space between the first vessel portion a and the secondvessel portion b is completely blocked. As a result, the accommodatedsubstance in the vessel is divided in two.

In the case of this example, the step (ii) and the step (iii) are oftenperformed at the same time. In this case, the self-fusing material canbe extended and twisted off by applying, as an external force, theresultant of a twisting force around an axis in a direction in which thefirst vessel portion a and the second vessel portion b are pulled awayfrom each other and a pulling force in the direction of the axis.

Another example of the method is as follows. As shown in FIG. 4(iii),the self-fusing material X, whose surface has high self-fusibility,between the first vessel portion a and the second vessel portion b mayalso be externally pinched to form a pressure-bonded surface. In thiscase, in FIG. 4(iii), the self-fusing material X whose surface has highself-fusibility is fused together by pressure bonding using twopressure-bonding members 31 so that the space between the first vesselportion a and the second vessel portion b is completely blocked. Thismakes it possible to divide the accommodated substance in the vessel intwo. It is to be noted that an example of pressure-bonding means havingtwo pressure-bonding members 31 as shown in FIG. 4(iii) includes a jigwith a pinching function such as a pair of pliers.

In the step (iv), a fused part of the self-fusing material is cut.

In the case of an embodiment shown in FIG. 3, as shown in FIG. 3(iv), aself-fused part of the self-fusing material X between both the vesselportions a and b can be twisted off by further twisting (turning) boththe vessel portions a and b. In this case, the self-fused part can beeasily twisted off by twisting both the vessel portions a and b whilefurther pulling both the vessel portions away from each other.

On the other hand, in the case of an embodiment shown in FIG. 4, asshown in FIG. 4(iv), a self-fused part (pressure-bonded surface) of theself-fusing material X between both the vessel portions a and b can becut using cutting means 32. In this case, the pressure-bonded surfaceshall be cut at about its center.

In the case of a separation system illustrated in FIG. 4, the cuttingmeans 32 is prepared separately from the pressure-bonding members 31.That is, the cutting means 32 and the pressure-bonding members 31 can beseparately used as means and members different in function (eithercutting or pressure-bonding), respectively.

On the other hand, as a modified embodiment, the cutting means may beprepared together with the pressure-bonding members so that theseparation system has both the functions of cutting andpressure-bonding. A specific example thereof is shown in FIG. 5. Thecutting means 32 of a separation system illustrated in FIG. 5 includes acutter main body 41, whose part including a cutting edge 42 is slidablyaccommodated in one of the pressure-bonding members 31L, and apressurizing head 43 provided at the opposite end from the cutting edge42. A spring 44 is provided between the pressurizing head 43 and thepressure-bonding member 31L. In the other pressure-bonding member 31R, arecess 45 that can receive the cutting edge 42 is provided.

In the case of an embodiment shown in FIG. 5, the self-fusing material Xis extended in the step (ii) (FIG. 5(ii)), and the extended self-fusingmaterial X is pinched between the pressure-bonding members 31L and 31Rby pressing the pressurizing head 32 in the direction of an arrow toform a pressure-bonded surface in the step (iii) (FIG. 5(iii)). In thestep (iv), the pressurizing head 43 is further pressed so that thecutter main body 41 is slidably moved within the pressure-bonding member31L, and the cutting edge 42 reaches and cuts the pressure-bondedsurface of the self-fusing material X, and then reaches the recess 45 ofthe pressure-bonding member 31R (FIG. 5(iv).

In the case of the embodiment shown in FIG. 5, unlike the embodimentshown in FIG. 4, the vessel can be separated by the simple operation ofonly pressing in one direction. Further, the separation systemillustrated in FIG. 5 is a simple system by which cutting is performedsimply by pressing, and therefore can be miniaturized. Therefore, forexample, even when two or more vessels are integrated in series or in amatrix, these structures can be treated collectively by a single action.

In the above cutting step, separated structures can be obtained from thevessel in a state where the fracture openings 11 a and 11 b arecompletely closed. Specifically, as shown in FIGS. 3(iv), 4(iv), and5(iv), a first separated structure is obtained which includes the firstvessel portion a, whose fracture opening 11 a is closed by a self-fusingmaterial X_(a), and contains one separated part of the accommodatedsubstance, and a second separated structure is obtained which includesthe second vessel portion b, whose fracture opening 11 b is hermeticallysealed by a self-fusing material X_(b), and contains the other separatedpart of the accommodated substance. The fracture openings 11 a and 11 b,formed by separation, of the respective separated structures are bothcompletely sealed at the same time by a membrane of the extendedself-fusing material. That is, leakage or slipping of the accommodatedsubstance does not occur in the separated structure of the first vesselportion a-side, and the accommodated substance in the separatedstructure of the second vessel portion b-side is completely hermeticallysealed.

In this way, part of the vessel can be separated without bringing theaccommodated substance to be collected into contact with an outsideatmosphere.

As illustrated in FIG. 3(v), the accommodated substance can be reliablytaken out from the separated structure without contact with an outsideatmosphere or in a safe place by sucking out the accommodated substancethrough a fine-tipped micropipette chip 21 or an injection needlepenetrating a membrane of the self-fusing material X_(b).

Another modified embodiment of the present invention is shown in FIG. 6.The embodiment shown in FIG. 6 is applied with the embodiment shown inFIG. 4, and is provided with two portions (between a vessel portion aand a vessel portion b and between the vessel portion b and a vesselportion c) to be connected. This makes it possible to collect only amiddle part of the vessel (the vessel portion b and a substanceaccommodated therein). For example, it is possible to take out only aspecific band in a column. This embodiment is useful in that a band thatbecomes undesirably broad as the retention time on a column increasescan be fractionated in a sharp state. Similarly, more portions to beconnected can also be provided. In the embodiment illustrated in FIG. 6,cutting is performed by the method shown in FIG. 3, but of course,cutting may be performed by the separation system shown in FIG. 4 or 5.

[4. Accommodated Substance in Vessel-Shaped Structure (ManipulationVessel)]

A substance to be accommodated in the vessel of the present invention isnot particularly limited, and one or more are arbitrarily selected fromthe group consisting of a liquid, a solid, a gas, and a dispersionsystem.

The liquid may be either an aqueous liquid or a non-aqueous liquid. Asfor the dispersion system, a dispersion medium and a dispersoid used incombination may each be any one of a solid, a liquid, and a gas.Specific examples of the dispersion system include a gel (which may beeither a hydrogel or an oil gel), a sol, and a slurry of a fillingmaterial for chromatography and a developing solvent.

The vessel of the present invent ion may be preferably used to subjectan object component to manipulation therein. That is, the vessel of thepresent invention is used as a manipulation vessel.

In this case, the object component is not particularly limited as longas the object component is a component that can be manipulated in aliquid, a solid, a gas, and a dispersion system. Therefore, the objectcomponent may be either a natural product or a non-natural product, andmay be either an in-vivo component or an in-vitro component.

A substance to be accommodated in the manipulation vessel includes amanipulation medium as a field for performing manipulation to which anobject component is to be subjected. The manipulation of the objectcomponent includes subjecting the object component to treatment in theabove-described accommodated substance and transporting the objectcomponent in the accommodated substance. The treatment to which theobject component is to be subjected includes treatment accompanied by achange of the object component into another substance (e.g., chemicalreaction and biochemical reaction) and treatment accompanied by aphysical change of the object component (e.g., denaturation,dissolution, mixing, emulsification, and dilution of the objectcomponent). Processes such as extraction, purification, synthesis,elusion, separation, collection, and analysis of the object componentcan be performed by these treatments. More specifically, when the objectcomponent is, for example, nucleic acid contained in a nucleicacid-containing sample (e.g., tissue, body fluid, excrement), treatmentssuch as nucleic acid extraction, nucleic acid washing, nucleic acidisolation, and a nucleic acid amplification reaction can be performed.

[4-1. Case of Column for Chromatography]

When the manipulation vessel is a column for chromatography (which mayhave a shape illustrated in FIG. 1(1)), examples of the manipulationmedium include a filling material for chromatography and a developingsolvent (hereinafter, these may be sometimes simply referred to as afilling material for chromatography). As shown in FIG. 1(1), the fillingmaterial for chromatography 3 c may be accommodated in the manipulationvessel portion a. Further, a filter 3 s may be accommodated so as to belocated at the lower end of the filling material for chromatography 3 c.The collection vessel portion b may accommodate nothing as shown in FIG.1(1) or may accommodate a liquid or the like to be mixed with a fractioncontaining an object component.

Examples of the filling material for chromatography includereverse-phase CDS and a gel filtration carrier, but the filling materialfor chromatography is not limited thereto and can be appropriatelyselected by those skilled in the art. The developing solvent and acollection liquid are also appropriately selected by those skilled inthe art.

[4-2. Case of Manipulation Tube Device (Capillary Microdevice)]

When the manipulation vessel is a tubular-shaped vessel illustrated inFIG. 1(2), an example of the manipulation medium is a multi-layeredobject in which layers of an aqueous liquid and a gel are alternatelystacked in a longitudinal direction. More specifically, the lowermostlayer of the multi-layered object accommodated in the manipulationvessel portion a is usually the gel layer 2, and the liquid layers 3 land the gel layers 3 g are alternately stacked on the gel layer 2. Anaccommodated substance 4 in the collection vessel portion b may beeither an aqueous liquid or a gel.

As the aqueous liquid, one required to perform the above-describedtreatment can be appropriately selected by those skilled in the art. Inthe above-exemplified case where nucleic acid contained in a nucleicacid-containing sample is an object component to be subjected totreatment, examples of the aqueous liquid include a nucleic acidextraction liquid, a nucleic acid washing liquid, a nucleic acidisolation liquid, and a nucleic acid amplification reaction liquid.

On the other hand, the gel layers sandwich the aqueous liquid in themanipulation tube from both sides in the longitudinal direction of thetube to play a role as a plug (gel plug) fixing the aqueous liquid in apredetermined position in the tubs. The gel is comprised of achemically-inert substance that is insoluble or poorly-soluble in aliquid constituting the aqueous liquid layer when stacked together withthe aqueous liquid in the tube. The phrase “insoluble or poorly-solublein a liquid” means that the degree of solubility in the liquid at 25° C.is about 100 ppm or less.

The gel includes both an organogel and a hydrogel.

As the organogel, one prepared by gelling a water-insoluble or poorlywater-soluble liquid substance with the addition of a gelling agent maybe usually used. As the water-insoluble or poorly water-soluble liquidsubstance, an oil is used, whose degree of solubility in water at 25° C.is about 100 ppm or less and which is in a liquid state at ordinarytemperature (25° C.±15° C.). For example, one or a combination of two ormore selected from the group consisting of liquid oils and fats, esteroils, hydrocarbon oils, and silicone oils may be used. As the gellingagent, one or a combination of two or more oil-gelling agents selectedfrom the group consisting of hydroxy fatty acids, dextrin fatty acidesters, and glycerin fatty acid esters may be used.

The amount of the gelling agent added to the liquid substance may be,for example, 0.1 to 0.5 wt %, 0.5 to 2 wt %, or 1 to 5 wt % of the totalweight of the liquid substance. A gelling method can be appropriatelydetermined by those skilled in the art.

As the hydrogel, one prepared by equilibrium swelling of a hydrogelmaterial in water or an aqueous liquid may be used. Examples of thehydrogel material include gelatin, collagen, starch, pectin, hyaluronicacid, chitin, chitosan, alginic acid, and derivatives thereof.

As in the case of the above-described aqueous liquid, when the hydrogelis one that provides an environment for treatment to which an objectcomponent is to be subjected (as one example, the hydrogel is a DMAhydrogel (P-gel) that provides a reaction environment for obtaining aprotein from an object component when the object component is asubstrate for protein synthesis), such a hydrogel is appropriatelyprepared by those skilled in the art so as to have composition suitablefor such treatment,

The multi-layered object may be accommodated in at least themanipulation vessel portion a. As will be described later, the aqueousliquid forming an uppermost layer may further contain magneticparticles. In the collection vessel portion b, a substance suitable forcollecting an object component (which is selected from the groupconsisting of a liquid, a solid, a gas, and a dispersion system) isaccommodated.

The rough inner diameter of a tube constituting the manipulation tubeis, for example, 0.1 mm to 5 mm, preferably 1 to 2 mm from the viewpointof ensuring excellent manipulability, but is not limited thereto. Thelength in longitudinal direction of the tube is, for example, 1 to 30cm, preferably 5 to 15 cm. The multi-layered object is accommodated inthe tube having such sixes by forming a desired number of layers in amanner that gel plugs having a thickness of, for example, 1 to 20 mm,preferably 2 to 5 mm are contained.

[4-3. Case of Droplet Manipulation Device]

When the manipulation vessel has a shape illustrated in FIG. 2, anaqueous liquid added thereto is sunk as the droplet 3 d in the dropletencapsulating medium 5, and accommodated in the vessel, if the specificgravity of the droplet encapsulating medium 5 in which a sol-geltransition function is given to the above-described water-insoluble orpoorly water-soluble liquid substance is less than 1. The droplet can bemade movable or immovable by controlling the temperature of the dropletencapsulating medium 5 with the use of its sol-gel transitiontemperature as a border. Further, a recess may be formed in the surfaceof the gel-state droplet encapsulating medium to hold the droplet 3 d′of an aqueous liquid in the recess.

The amount of the aqueous liquid constituting one droplet 3 daccommodated in the vessel is not particularly limited, but is, forexample, about 0.1 to 20 μL.

The amount of the droplet encapsulating medium 5 accommodated in thevessel is not particularly limited as long as the amount is sufficientto completely encapsulate the droplet 3 d. Specifically, the dropletencapsulating medium, whose volume is 1.0 times to 10,000 times, or1,000 times to 50,000 times that of the droplet, can be used.

As will be described later, the aqueous droplet 3 d′ accommodated in thevessel may further contain magnetic particles.

[5. Example of Use of Device Using Manipulation Vessel]

[5-1. Case of Column for Chromatography]

As shown in FIG. 4, an impurity-containing object substance sampleliquid 30 charged through the sample supply portion 12 is fractionatedby the filling material for chromatography 3 c in the manipulationportion A, and a fraction of an object component is filtered through thefilter 3 s and a filtrate is dropped into the collection portion B. Ahermetically-sealed air layer is present between the filter 3 s and thecollection liquid 4, and therefore after the filtrate is dropped intothe collection portion to some extent, the amount thereof is stopped ata predetermined level due to an increase in the internal pressure of thecollection portion B. (If the manipulation portion A and the collectionportion B are separated from each other not by the method according tothe present invention, a filtrate immediately starts to drop again fromthe filter due to atmospheric pressure. If the filtrate is derived froma fraction containing impurities, the impurities flow into thecollection portion B.)

Then, as shown in FIGS. 4(i) to 4(iv) the filtrate can be collected byseparating the collection portion B from the column by the methodaccording to the present invention.

[5-2. Case of Manipulation Vessel Using Magnetic Particles]

Hereinbelow, a device using a manipulation tube as the manipulationvessel (capillary microdevice) and a device using a rectangular (ordeformed rectangular) vessel as the manipulation vessel (dropletmanipulation device) will be described. In each of the devices,manipulation such as capture or transport of an object component can beperformed by adsorbing the object component to magnetic particles andfluctuating a magnetic field from the outside of the manipulation vesselwith the use of magnetic field applying means.

The magnetic particles are used to move an object component in themanipulation vessel together with a small amount of liquid lump to beaccompanied by moving a magnetic field from the outside of themanipulation vessel. The magnetic particles usually have a chemicalfunctional group on the surface thereof. The magnetic particles may beaccommodated in the manipulation vessel in advance, or may not beaccommodated in the manipulation vessel in advance. When the magneticparticles are accommodated in the manipulation vessel in advance, forexample, magnetic particles 61 may be previously contained in anuppermost aqueous liquid layer 3 g ₁ as shown in FIG. 7, or may bepreviously contained in an aqueous liquid present nearest the samplesupply portion, such as an aqueous droplet 3 d′ placed on a dropletencapsulating medium 5 g, as shown in FIG. 8.

On the other hand, when not accommodated in the manipulation vessel inadvance, the magnetic particles are supplied into the manipulationvessel in the state of being mixed with a sample containing an objectcomponent.

The magnetic particles are not particularly limited as long as they areparticles that respond to magnetism. Examples thereof include particleshaving a magnetic material such as magnetite, γ-iron oxide, or manganesezinc ferrite. Further, the magnetic particles may have a surface havinga chemical structure specifically binding to a target component to besubjected to the above-described treatment or reaction, such as an aminogroup, a carboxyl group, an epoxy group, avidin, biotin, digoxigenin,protein A, protein G, a complexed metal ion, or an antibody or may havea surface specifically binding to a target component by electrostaticforce or van der Waals force. This makes it possible to selectivelyadsorb a target component to be subjected to reaction or treatment tothe magnetic particles.

Examples of a hydrophilic group on the surface of the magnetic particlesinclude a hydroxyl group, an amino group, a carboxyl group, a phosphoricgroup, and a sulfonic group.

The magnetic particles may further contain, in addition to the aboveelements, various elements appropriately selected by those skilled inthe art. Preferred specific modes of the magnetic particles having ahydrophilic group on their surface include particles composed of amixture of a magnetic material and silica and/or an anion exchangeresin, magnetic particles whose surfaces are coated with silica and/oran anion exchange resin, magnetic particles whose surfaces axe coatedwith gold having a hydrophilic group binding thereto through a mercaptogroup, and gold particles containing a magnetic material and having ahydrophilic group binding to their surface through a mercapto group.

The average particle size of the magnetic particles having a hydrophilicgroup on their surface may be about 0.1 μm to 500 μm. When the averageparticle size is small, the magnetic particles are likely to be presentin a dispersed state in the aqueous liquid layer when freed from amagnetic field.

The magnetic field applying means that causes the movement of a magneticfield for moving the magnetic particles in the manipulation vesseltogether with an object component is not particularly limited. As themagnetic field applying means, a magnetic force source such as apermanent magnet (e.g., a ferrite magnet or a neodymium magnet) or anelectromagnet can be used. The magnetic field applying means can bearranged outside of and close to the manipulation vessel to the extentthat the magnetic particles dispersed in the aqueous liquid layer ordroplet in the manipulation vessel can be aggregated on the inner wallsurface (transfer surface) of the manipulation vessel, and that theaggregated magnetic particles in the gel layer or droplet encapsulatingmedium in the manipulation vessel can be transported while remaining inan aggregation state. This makes it possible for the magnetic fieldapplying means to effectively produce a magnetic field for the magneticparticles in a state where the transfer surface of the manipulationvessel is interposed between the magnetic particles and the magneticfield applying means, thereby allowing an object component to becaptured and transported together with the aggregated magneticparticles.

Further, the magnetic particles can be moved even in a gel by externallyoperating a magnetic field, and therefore can pass through the gel. Thisis due to the thixotropic properties (thixotropy) of the gel. That is,the magnetic particles in the manipulation vessel give a shear force tothe gel along the transfer surface by externally moving a magnet, andthe gel in front of the magnetic particles in the direction in which themagnetic particles are moved is fluidized by solation so that themagnetic particles can be moved directly. Further, after the passage ofthe magnetic particles, the sol freed from the shear force isimmediately returned to a gel state, and therefore a through hole is notformed in the gel by the passage of the magnetic particles. By utilizingsuch a phenomenon, an object substance can be easily moved usingmagnetic particles as a carrier, and therefore, for example, it ispossible to perform switching among various chemical environments towhich the object substance is to be subjected and which is created bydroplets in a very short time.

[5-2-1. Case of Manipulation Tube Device (Capillary Microdevice)]

As an example of use of a manipulation tube, a method (FIG. 7) will bedescribed below, in which nucleic acid is extracted from a biologicalsample containing nucleic acid as an object component, and washed in amanipulation tube. Means for subjecting an object component other thannucleic acid to a desired manipulation can be appropriately selected bythose skilled in the art with reference to the following example.

In a manipulation tube shown in FIG. 7, a multi-layered object, in whicha cell lysis liquid (containing a surfactant and a chaotropic salt suchas guanidine thiocyanate) 3 l ₁ and washing liquids 3 l ₂ to 3 l ₄ andgel plugs 3 g ₁ to 3 g ₃ and 2 g are alternately stacked, isaccommodated in a manipulation vessel portion a, and an eluent 4 isaccommodated in a collection vessel portion b with an air layerinterposed between the multi-layered object and the eluent 4.

In a manipulation portion A, a biological sample 30 containing an objectcomponent is supplied to the cell lysis liquid 3 l ₁ in the manipulationtube 1 through a sample supply portion 12 so that nucleic acid isisolated from cells (FIG. 7(1)). The isolated nucleic acid can bespecifically adsorbed to the silica surface of magnetic particles 61.The adsorbed nucleic acid is accompanied by reaction-inhibitingcomponents as it is, and therefore cannot be directly used as a templatefor gene amplification reaction. For this reason, the magnetic particlesaxe washed with the washing liquid 3 l ₂ while the nucleic acid remainsadsorbed to the surface of the magnetic particles. At this time, inorder to prevent a large amount of the reaction-inhibiting componentsfrom being brought info the washing liquid, the magnetic particles 61are gathered by a magnet 63 (FIG. 7(2)) and are allowed to pass throughthe gel plug 3 g ₁ separating the cell lysis liquid 3 l ₁ and thewashing liquid 3 l ₂ from each other (FIG. 7(3)). By allowing themagnetic particles to pass through the gel plug 3 g ₁, the magneticparticles can reach the washing liquid 3 l ₂ together with few liquidfractions (FIG. 7(4)). Therefore, the magnetic particles can be highlyefficiently washed. Further, by repeating the passage of the magneticparticles through the gel plug (3 g ₂, 3 g ₃) and the transport of themagnetic particles to the washing liquid (3 l ₃, 3 l ₄) (FIGS. 7(5) to7(10)), the degree of purification of the nucleic acid can be increased.The nucleic acid purified while remaining adsorbed to the surface of themagnetic particles is again gathered by the magnet (FIG. 7(11)), allowedto pass through the gel plug 2 g (FIG. 7(12)), and transported into theeluent 4 (FIG. 7 (13)). In the eluent 4, the nucleic acid is separatedfrom the magnetic particles and eluted. When contamination of themagnetic particles into a collected substance is not desired, forexample, the magnetic particles, from which the nucleic acid has beenelated, are again stayed in the gel plug 2 g, and the elated purifiednucleic acid remains in the collection portion B (FIG. 7 (14)). The thusobtained nucleic acid is useful as template nucleic acid that can beanalyzed by a nucleic acid amplification reaction. The obtained nucleicacid can be collected in a completely hermetically-sealed state bydetaching the collection portion B from the manipulation portion A ofthe manipulation tube by the separation method according to the presentinvention (FIG. 7(15)). The collected nucleic acid can be subjected tothe next manipulation (process of performing analysis by a nucleic acidamplification reaction).

In a modified embodiment of the above embodiment, any one of theaccommodated substances in the manipulation tube (e.g., the washingliquid 3 l ₄ or the eluent 4) may be changed to a nucleic acidamplification liquid. In this case, the extracted and washed nucleicacid can be amplified by subjecting the nucleic acid amplificationliquid to appropriate temperature cycles with the use of appropriateheating means. The amplified nucleic acid can be collected in acompletely hermetically-sealed state by detaching the collection portionB from the manipulation portion A by the separation method according tothe present invention.

[5-2-2. Case of Droplet Manipulation Device]

As an example of a droplet manipulation device, a method (FIG. 8) willbe described below, in which nucleic acid is extracted from a biologicalsample containing nucleic acid as an object component, washed, andamplified in a manipulation tube. Means for subjecting an objectcomponent other than nucleic acid to a desired manipulation can beappropriately selected by those skilled in the art with reference to thefollowing example.

A device shown in FIG. 8 can be prepared in the following manner. Aheated mixture (e.g., 90° C.) of, for example, a silicone oil and anoil-gelling agent is filled into a vessel to have a filling height of,for example, about 3 mm. After the temperature of the heated mixture isreduced (e.g., 60° C.), one droplet 3 d ₁ of a nucleic acid extractionliquid, two droplets 3 d ₂ and 3 d ₂ of a washing liquid, and onedroplet 3 d ₄ of a PCR reaction liquid are placed in the oil, and theoil is allowed to stand until its temperature is reduced to roomtemperature so that the entire oil can be gelled. Further, a recess canbe formed in the surface of the gelled oil to place a mixture 3 d′ of acell lysis liquid containing magnetic silica particles and a nucleicacid-containing biological sample in the recess.

After the vessel is covered, the end of an alumina ceramic plate (notshown) is separately heated with an electric heater. At the time when atemperature gradient is stably created on the surface of the plate, thevessel is placed on the plate and allowed to stand. In this way, part(left half in FIG. 8) of the gel in the vessel is solated by heat, andtherefore both a gel 5 g having no fluidity and a sol 5 s havingfluidity coexist as a droplet encapsulating medium.

As shown in FIG. 8(a), since the droplet encapsulating medium 5 g is ina gel state having no fluidity, the magnetic particles 61 can beseparated toward a transfer surface direction by bringing the magneticforce source (magnet) 63 close to the vessel 1 to generate a magneticfield in a direction from the transfer surface side toward the droplet 3d′ on the droplet encapsulating medium 5 g, while the droplet 3 d′remains placed on the droplet encapsulating medium 5 g. At this time,the magnetic particles 61 to be separated form an aggregate by amagnetic force, and the aggregated magnetic particle group accompanies asubstance adsorbed thereto and a small amount of liquid adhered aroundthereto. In other words, when the droplet 3 d′ is regarded as a maindroplet, a small droplet 71 b containing the magnetic particles isseparated. The separated small droplet 71 b is moved through the dropletencapsulating medium 5 g while breaking the tertiary structure of thegel under the guidance of a magnetic field, and therefore can be sunk tothe transfer surface of the vessel.

As shown in FIG. 8(b), the small droplet 71 b containing the magneticparticles and nucleic acid and other components attached thereto ismoved through the droplet encapsulating medium 5 g, and coalesced withanother encapsulated droplet 3 d ₁ comprised of a nucleic acidextraction liquid (FIG. 8 (c)), which makes it possible to extract anucleic acid component contained in the small droplet 71 b. Further, asshown in FIGS. 8(d) and 8(e), the extracted nucleic acid, which isaccompanied with the magnetic particles together with a smell droplet 71e, is separated from an encapsulated droplet 71 c comprised of thenucleic acid extraction liquid coalesced with the small droplet 71 b,and is moved into the droplet encapsulating medium 5 g by fluctuating amagnetic field.

Similarly in the case of performing washing treatment, the magneticparticles can be washed by moving the small droplet 11 e through theencapsulating medium 5 g and coalescing the small droplet with theencapsulated droplet 3 d ₂ comprised of a washing liquid. By washing themagnetic particles, the nucleic acid adsorbed to the magnetic particlescan be washed. Further, the washed nucleic acid, which is accompaniedwith the magnetic particles together with a small droplet, is separatedfrom the encapsulated droplet comprised of a washing liquid, and ismoved into the encapsulating medium by fluctuating a magnetic field.Similarly, the magnetic particles can be washed again by coalescing thesmall droplet with another encapsulated droplet 3 d ₃ comprised of awashing liquid.

The nucleic acid-containing sample or a small droplet 71 f subjected tothe above-described nucleic acid extraction treatment and washingtreatment, if necessary, is coalesced with the droplet 3 d ₄ comprisedof a nucleic acid amplification liquid (FIGS. 8(f) and 8(g)). This makesit possible to obtain a droplet 71 g comprised of the nucleic acidamplification liquid containing the nucleic acid to be amplified and themagnetic particles. The droplet encapsulating medium 5 s surrounding thedroplet 3 d ₄ is in a sol state having fluidity, and therefore theentire droplet 71 g obtained by coalescence with the droplet 71 f can bemoved. A nucleic acid amplification reaction can be started by movingthe droplet 71 g to a point of a nucleic acid amplification reactioninitiation temperature in a temperature variable region (FIG. 8(h)).

After the completion of the nucleic acid amplification reaction, asshown in FIG. 8(i), a droplet 71 i containing an amplified product ismoved into the collection portion B, and the amplified product can becollected in a completely hermetically-sealed state by detaching thecollection portion B from the manipulation portion A by the separationmethod according to the present invention.

EXAMPLES Experimental Example 1

A vessel 1 shown in FIG. 9 was prepared. Specifically, afracture-inducing groove 6 was formed by notching a polypropylenecapillary (outer diameter: 4 mm, inner diameter: 2 mm) in a positionwhere the capillary should be separated (position where fracture shouldbe caused). The fracture-inducing groove was formed to have a crosssection having a V shape with an angle of 60° and a depth of d. A vesselportion a of the vessel 1 was fixed by a fixture 91, and a vesselportion b was fixed by a fixture 92. At this time, the fixation wasperformed in such a manner that the length from the lower end of thefixture 91 to the deepest point of the fracture-inducing groove 6 was 95mm, and the length from the upper end of the fixture 92 to the deepestpoint of the fracture-inducing groove 6 was 5 mm. The fixture 91 wasfixed so as not to turn. On the other hand, the fixture 92 was connectedto a motor, and a rotational torque was applied to the fixture 92 tocause fracture in the fracture-inducing groove 6. As a result, thevessel 1 was separated into the vessel portion a and the vessel portionb.

A relationship between the depth d of the fracture-inducing groove andthe rotational torque causing the capillary to be separated due tostress concentration on the fracture-inducing groove is shown in FIG.10. As can be seen from the results, conditions such that fracture inthe fracture-inducing groove due to stress concentration is caused whena rotational torque of 8 to 11 cN·m is applied at a depth of 0.3 to 0.5mm are particularly suitable in this experimental example. The aboveranges are optimal ranges in which the toughness of the capillary as avessel device is not impaired and fracture cannot be easily causedmanually but fracture and separation can be mechanically caused withhigh reproducibility.

Experimental Example 2

A fracture-inducing zone was formed in a polypropylene capillary (outerdiameter: 4 mm, inner diameter: 2 mm) in a position where the capillaryshould be separated (position where fracture should be caused) in thefollowing manner. Seventy percent (v/v) concentrated nitric acid wasapplied with a width of 2 mm onto the outer peripheral surface of thecapillary in a position where the capillary should be separated, and wasthen heated at 70° C. for 1 hour to denature polypropylene from theapplication surface toward the inside of a vessel wall. The manipulationof applying and heating concentrated nitric acid was repeated untilyellowing due to denaturation finally reached the midpoint of the vesselwall in the thickness direction thereof.

The fracture-inducing zone was washed, and was then wrapped and coveredwith butyl rubber. In this way, a separable vessel was prepared.

The invention claimed is:
 1. A manipulation device for manipulating anobject component in a vessel, comprising: the vessel which is aseparable vessel comprising: a fracture-inducing portion formed in aposition where fracture should be caused to separate the vessel into afirst vessel portion and a second vessel portion; and a self-fusingmaterial provided on an outer surface so as to cover thefracture-inducing portion, and the vessel containing an accommodatedsubstance therein; magnetic particles that should capture and transportan object component; and a magnetic field application member forapplying a magnetic field to the vessel so that the magnetic particlescan be moved from an inside of the first vessel portion to an inside ofthe second vessel portion, wherein the fracture-inducing portion has areduced wall thickness and/or a reduced material strength as comparedwith the rest of the vessel; and wherein the magnetic field applicationmember is a permanent magnet or an electromagnet.
 2. The manipulationdevice according to claim 1, the vessel being a manipulation vessel forsubjecting a sample containing an object component to a predeterminedmanipulation therein, wherein the first vessel portion is a manipulationportion for subjecting a sample containing an object component to apredetermined manipulation, the second vessel portion is a collectionportion for collecting a target substance from the manipulation portion,and the accommodated substance is a manipulation medium selected fromthe group consisting of a liquid, a solid, a gas, and a dispersionsystem, as a field for performing manipulation to which the objectcomponent is to be subjected.
 3. The manipulation device according toclaim 2, wherein the manipulation portion comprises a column forchromatography, and the manipulation medium comprises a filling materialfor chromatography and a developing solvent.
 4. The manipulation deviceaccording to claim 2, the vessel having a tubular shape, wherein themanipulation medium is a multi-layered object in which layers of anaqueous liquid and a gel are alternately stacked in a longitudinaldirection.
 5. The manipulation device according to claim 2, wherein themanipulation medium comprises a droplet encapsulating medium and anencapsulated aqueous droplet.
 6. The manipulation device according toclaim 1, wherein the vessel further comprises a protective member on anouter surface of the self-fusing material.
 7. The manipulation deviceaccording to claim 1, wherein the self-fusing material has a thicknessof 0.01 to 5 mm per 1 cm² of area of a plane within an outer peripheryof the vessel.
 8. The manipulation device according to claim 1, whereinthe self-fusing material is selected from the group consisting ofisobutylene-isoprene copolymers, ethylene-propylene-diene copolymers,polyisobutylene, paraffin, polyvinyl acetate, polyurethane, polydimethylsiloxane, ethylene propylene copolymers, hydrogel polymers,(meth)acrylic acid ester copolymers, silicone rubber, and naturalrubber.
 9. The manipulation device according to claim 1, wherein theself-fusing material is a thermoplastic resin having a glass transitiontemperature of 50° C. to 180° C.
 10. The manipulation device accordingto claim 9, wherein the thermoplastic resin is selected from the groupconsisting of polyethylene, polypropylene, polystyrene, ethylene-vinylacetate copolymers, polyacetal, polymethyl methacrylate, polyvinylalcohol, polyvinyl chloride, vinyl chloride-vinyl acetate copolymers,vinyl chloride-acrylic acid ester copolymers, polyvinylidene chloride,and vinylidene chloride-acrylic acid ester copolymers.